Evidence map›Paper›PMID 31482479›Full record

ReviewCurrent treatment options in oncology2019

Diagnosis and Treatment of ALK Aberrations in Metastatic NSCLC.

Alex Friedlaender, Giuseppe Banna, Sandip Patel, Alfredo Addeo

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current treatment options in oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  18. Targeted Therapies in Early Stage NSCLC: Hype or Hope?International journal of molecular sciences · 2020
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Alex FriedlaenderOncology Department, Geneva University Hospital (CH), Rue Gabrielle-Perret-Gentil 4, 1205, Genève, Switzerland.
Giuseppe BannaDivision of Medical Oncology, Cannizzaro Hospital, Catania, Italy.
Sandip PatelSandip Pravin Patel, UC San Diego Moores Cancer Center, 3855 Health Sciences Dr, La Jolla, CA, 92037, USA.
Alfredo AddeoOncology Department, Geneva University Hospital (CH), Rue Gabrielle-Perret-Gentil 4, 1205, Genève, Switzerland. alfredo.addeo@hcuge.ch.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

opinion statementThere has been rapid progress in the use of targeted therapies for ALK-positive which has led to improve dramatically PFS and OS in the metastatic ALK-rearranged NSCLC patients. There are several molecules now available (crizotinib, ceritinib, brigatinib, alectinib, and lorlatinib) and others in development. Such an improvement in treatment efficacy has even more highlighted the importance of an adequate identification of ALK alterations. Efficient and easily accessible testing tools are required to identify eligible patients in a timely fashion. Different methods for detecting ALK+ NSCLC patients are now available, with fluorescence in situ hybridization (FISH) and immunohistochemistry (IHC) currently representing validated diagnostic techniques for the initial assessment of ALK status. Furthermore the widespread use of next-generation sequencing to detect other possible different activating mutations has allowed to identify individual ALK fusion variants. Several more expensive and time-consuming methods are also available nowadays which have the advantage to detect even rarer uncommon ALK fusion variants and mutations in tumour or blood samples. A review of the evolving testing-treatment landscape is needed to highlight the importance of properly diagnosing and treating this group of patients.

Indexed as

Chromosome AberrationsAnaplastic Lymphoma KinaseBiomarkers, TumorCarcinoma, Non-Small-Cell LungDisease ManagementHumansLiquid BiopsyLung NeoplasmsMolecular Diagnostic TechniquesMolecular Targeted TherapyNeoplasm MetastasisNeoplasm StagingProtein Kinase InhibitorsALK protein, humanAnaplastic Lymphoma KinaseBiomarkers, TumorProtein Kinase InhibitorsALK aberrationNSCLCTesting

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.